| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/NG.3652 |
| P698 | PubMed publication ID | 27573686 |
| P2093 | author name string | Onur Emre Onat | |
| Tayfun Özçelik | |||
| P2860 | cites work | Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol | Q22337068 |
| Linkage of early-onset familial breast cancer to chromosome 17q21 | Q28268902 | ||
| Genetic heterogeneity in human disease | Q28280100 | ||
| Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease | Q34792986 | ||
| Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome | Q35200261 | ||
| Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery | Q37250132 | ||
| Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network | Q37487752 | ||
| Reverse genetics and human disease | Q38168782 | ||
| Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair | Q50668042 | ||
| Collaborative genomics for human health and cooperation in the Mediterranean region | Q57499928 | ||
| Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1 | Q77931822 | ||
| P433 | issue | 9 | |
| P304 | page(s) | 978-979 | |
| P577 | publication date | 2016-08-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Genomic landscape of the Greater Middle East | |
| P478 | volume | 48 |
| Q48120253 | A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features. |
| Q52647099 | Incidental and clinically actionable genetic variants in 1005 whole exomes and genomes from Qatar |
| Q41696409 | Medical genetics and genomic medicine in Turkey: a bright future at a new era in life sciences |
| Q34554954 | Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder |
| Q38714900 | al mena: a comprehensive resource of human genetic variants integrating genomes and exomes from Arab, Middle Eastern and North African populations |
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